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Clinical controlled study for computer-aided cognitive assessment and training system based on PASS theory for patients with post stroke cognitive impairment

Clinical controlled study for computer-aided cognitive assessment and training system based on PASS theory for patients with post stroke cognitive impairment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018633
Enrollment
Unknown
Registered
2018-09-30
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cognitive impairment

Interventions

Experimental group: routine cognitive training and cognitive training based on PASS
Control group: two routine cognitive training sessions

Sponsors

China Rehabilitation Research Center Dept. of Neurorehabilitation(k2)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Comply with the diagnostic criteria of the Fourth National Cerebrovascular Conference Stroke, and confirmed by CT or MRI; MMSE score: primary school education level = 20 points, secondary school and above education level = 24 points, combined The clinical comprehensive judgment is definitely cognitive dysfunction after stroke; the age is 18-80 years old, the education level is primary school and above; the first onset, the course of disease is 1-6 months, the condition is stable, the consciousness is clear; at least one limb can be completed simply Computer operation; can remain seated for 30 minutes.

Exclusion criteria

Exclusion criteria: combined with other mental illnesses and severe neurological diseases; cognitive impairment caused by pre-stroke or other causes; combined with other serious heart, lung, renal insufficiency, severe liver function and malignancy Tumors, etc.; severe vision, hearing and speech disorders, impeding cognitive assessment; unable to cooperate with examinations and rehabilitation training; patients or their families refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Countries

China

Contacts

Public ContactSong Luping

China Rehabilitation Research Center Dept. of Neurorehabilitation(k2)

songluping882002@aliyun.com+86 13681388763

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026